Search results for "paroxysmal dyskinesia"

The MalaCard for "paroxysmal dyskinesia" has been retired.
Searching MalaCards for entries containing "paroxysmal dyskinesia"

223 hits were found for 'paroxysmal dyskinesia'

# Family MCID Name MIFTS Score
1
FML185 Familial Paroxysmal Kinesigenic Dyskinesia 19 7.754
2
c FML186 Familial Paroxysmal Nonkinesigenic Dyskinesia 17 6.165
3
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 44 5.720
4
GNR006 Generalized Epilepsy and Paroxysmal Dyskinesia 20 5.704
5
P PRX004 Paroxysmal Nonkinesigenic Dyskinesia 31 5.159
6
P EPS030 Episodic Kinesigenic Dyskinesia 1 27 4.135
7
c PRX024 Paroxysmal Nonkinesigenic Dyskinesia 2 10 4.016
8
GLT019 Glut1 Deficiency Syndrome 2 31 3.554
9
PRX022 Paroxysmal Choreoathetosis 25 3.030
10
PRX086 Paroxysmal Exertion-Induced Dyskinesia 11 2.919
11
P PRM011 Primary Ciliary Dyskinesia 58 0.479
12
P DYS154 Dystonia 64 0.250
13
MVM001 Movement Disease 54 0.239
14
P EPL164 Epilepsy 66 0.194
15
DRG016 Drug Induced Dyskinesia 21 0.194
16
ALR002 Al-Raqad Syndrome 36 0.177
17
P PRK057 Parkinson Disease, Late-Onset 72 0.158
18
BSL008 Basal Ganglia Disease 43 0.156
19
P HRT032 Heart Disease 76 0.151
20
HPT074 Hepatic Adenoma, Somatic 51 0.143
21
VND001 Vein Disease 52 0.142
22
HNM002 Hinman Syndrome 25 0.142
23
c CNT035 Central Nervous System Disease 59 0.137
24
MYL009 Myelodysplastic Syndrome 74 0.133
25
P NRV007 Nervous System Disease 71 0.132
26
P HML002 Hemolytic Anemia 60 0.130
27
AND005 Androgen Insensitivity Syndrome, Mild 16 0.117
28
P ATX004 Ataxia 53 0.114
29
P ENC018 Encephalopathy 59 0.112
30
c CRN175 Coronary Heart Disease 4 21 0.111
31
ADC005 Adcy5-Related Dyskinesia 9 0.110
32
CRB009 Cerebritis 38 0.109
33
c CRN214 Coronary Heart Disease 5 23 0.108
34
SLP005 Sleep Disorder 53 0.107
35
PRD011 Proud Syndrome 42 0.102
36
NRN002 Neuronitis 42 0.101
37
P CRN178 Coronary Heart Disease 6 24 0.098
38
STR067 Stroke, Ischemic 77 0.094
39
P BDD001 Budd-Chiari Syndrome 56 0.094
40
CHL071 Child Syndrome 58 0.092
41
KDS001 Kid Syndrome 53 0.092
42
c PND001 Pain Disorder 55 0.090
43
P TRM003 Tremor 54 0.090
44
EXF001 Exfoliation Syndrome 57 0.089
45
P PLN008 Peeling Skin Syndrome 47 0.089
46
VST004 Vestibular Disease 47 0.088
47
ATN002 Autonomic Nervous System Disease 47 0.087
48
ATR060 Atrial Standstill, Digenic 53 0.086
49
c PLN018 Peeling Skin Syndrome 2 35 0.086
50
INN002 Inner Ear Disease 50 0.084
51
WLF001 Wolff-Parkinson-White Syndrome 57 0.084
52
RTN023 Retinitis 49 0.083
53
DYS140 Dyskinesia, Familial, with Facial Myokymia 22 0.083
54
PHY002 Physical Disorder 44 0.082
55
VNT011 Ventricular Fibrillation, Familial, 1 43 0.082
56
CNT017 Central Nervous System Origin Vertigo 28 0.082
57
CSY001 C Syndrome 49 0.081
58
ADT003 Auditory System Disease 51 0.080
59
MTH009 Mouth Disease 63 0.080
60
P INF032 Infertility 61 0.080
61
DSS008 Disease of Mental Health 55 0.080
62
P HMP006 Hemiplegic Migraine 44 0.079
63
P PSD015 Pseudohypoparathyroidism 44 0.079
64
HYP056 Hypoglycemia 61 0.076
65
P AXN010 Axenfeld-Rieger Syndrome, Type 3 54 0.075
66
c EPS013 Episodic Kinesigenic Dyskinesia 2 8 0.074
67
ISC004 Ischemia 59 0.073
68
c BNG023 Benign Familial Infantile Epilepsy 41 0.073
69
c CHR096 Chronic Pulmonary Heart Disease 40 0.073
70
P PNM007 Pneumonia 66 0.071
71
MYC033 Myoclonus 41 0.071
72
P CRD011 Cardiomyopathy 67 0.071
73
P THR014 Thrombocytopenia 64 0.071
74
P HPT021 Hepatitis 70 0.070
75
RSP006 Respiratory System Disease 62 0.070
76
P MYP004 Myopathy 67 0.070
77
WST001 West Syndrome 61 0.070
78
SPS057 Spasticity 42 0.067
79
CNT097 Central Hypoventilation Syndrome, Congenital 60 0.067
80
c DYS169 Dystonia-12 51 0.067
81
P CRV039 Cervicitis 44 0.067
82
NSD001 Nose Disease 52 0.066
83
ATN005 Autonomic Dysfunction 45 0.066
84
P SZR006 Seizure Disorder 57 0.065
85
END072 Endotheliitis 42 0.064
86
P HYP086 Hypothyroidism 65 0.063
87
P GNR027 Generalized Peeling Skin Syndrome 22 0.063
88
PRP030 Purpura 59 0.062
89
P CRB042 Cerebellar Ataxia 64 0.061
90
DDN006 Duodenitis 44 0.061
91
P ESP024 Esophagitis 62 0.061
92
P SHR029 Short Syndrome 60 0.061
93
ACR041 Acromelic Frontonasal Dysostosis 46 0.061
94
CHR073 Choreatic Disease 40 0.061
95
INS001 Insulinoma 59 0.060
96
PYR013 Pyruvate Kinase Deficiency 58 0.060
97
WLL006 Wells Syndrome 56 0.060
98
GDS001 Good Syndrome 45 0.060
99
P AST005 Asthma 82 0.059
100
CHL067 Cholecystitis 56 0.059
101
P PNT019 Pontocerebellar Hypoplasia 37 0.059
102
P CRN211 Coronary Artery Disease 75 0.059
103
P EPS003 Episodic Ataxia 56 0.059
104
c THR092 Thrombophilia Due to Thrombin Defect 56 0.059
105
P HYP024 Hypoparathyroidism 52 0.059
106
MNR002 Meniere's Disease 50 0.059
107
CRN017 Coronary Thrombosis 48 0.059
108
HPR003 Heparin-Induced Thrombocytopenia 46 0.059
109
c DYS119 Dystonia 9 37 0.059
110
P ENC004 Encephalitis 61 0.056
111
BRT030 Birth Defects 43 0.056
112
P HYP265 Hypotonia 39 0.056
113
OBS061 Obstructive Sleep Apnea 66 0.056
114
ATH004 Athetosis 25 0.056
115
P MSC033 Muscle Disorders 52 0.055
116
MSC004 Muscle Tissue Disease 36 0.055
117
P INT063 Intellectual Disability 53 0.055
118
c PLN017 Peeling Skin Syndrome 1 33 0.055
119
c PLN021 Peeling Skin Syndrome 3 31 0.055
120
P SLP006 Sleep Apnea 61 0.052
121
PLM033 Pulmonary Embolism 59 0.052
122
P MGR003 Migraine with Aura 51 0.052
123
SPL006 Splenic Infarction 35 0.052
124
P HLT001 Holt-Oram Syndrome 58 0.050
125
CLC006 Calcinosis 49 0.050
126
P BLD051 Blood Coagulation Disease 45 0.050
127
WTH001 Withdrawal Disorder 41 0.050
128
ADP007 Adie Pupil 34 0.050
129
P BPL003 Bipolar Disorder 62 0.049
130
P BLP003 Blepharospasm 44 0.049
131
ADR009 Adrenal Cortex Disease 41 0.049
132
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.049
133
PRP027 Peripheral Vascular Disease 69 0.047
134
P ALX003 Alexander Disease 64 0.047
135
c ACT075 Acute Myocardial Infarction 60 0.047
136
c ATM010 Autoimmune Hemolytic Anemia 60 0.047
137
P ANT006 Antiphospholipid Syndrome 58 0.047
138
P HMP007 Hemophilia 56 0.047
139
PTN001 Patent Foramen Ovale 54 0.047
140
BRN106 Burns 52 0.047
141
PRT018 Portal Vein Thrombosis 49 0.047
142
PPL021 Papilledema 48 0.047
143
LKC003 Leukocyte Disease 47 0.047
144
P RTN014 Retinal Artery Occlusion 43 0.047
145
BSL009 Basal Ganglia Calcification 43 0.047
146
P PRP034 Purpura Fulminans 42 0.047
147
CNT069 Centrotemporal Epilepsy 40 0.047
148
SPS019 Spastic Paraparesis 34 0.047
149
c STR089 Striatal Degeneration, Autosomal Dominant 2 30 0.047
150
HMD003 Hemidystonia 28 0.047
151
PSY012 Psychogenic Movement 22 0.047
152
CNS004 Constipation 57 0.043
153
DYS073 Dysphagia 49 0.043
154
MYL001 Myelitis 48 0.043
155
OBS015 Obesity, Hyperphagia, and Developmental Delay 46 0.043
156
CNT025 Central Pontine Myelinolysis 42 0.043
157
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 41 0.043
158
BLD054 Blood Protein Disease 40 0.043
159
GNC005 Geniculate Ganglionitis 31 0.043
160
c AST037 Asthma 1 31 0.043
161
PCK002 Pick Disease 67 0.042
162
TRN015 Transient Cerebral Ischemia 56 0.042
163
P THR005 Thrombotic Thrombocytopenic Purpura 55 0.042
164
THR004 Thrombocytosis 55 0.042
165
P THY032 Thyroiditis 54 0.042
166
INT075 Intracranial Hypertension 53 0.042
167
P LCT001 Lactic Acidosis 52 0.042
168
QDR001 Quadriplegia 52 0.042
169
OPT006 Optic Nerve Disease 51 0.042
170
HYP063 Hypersplenism 48 0.042
171
MDS022 Mediastinitis 41 0.042
172
PRP028 Peripheral Vertigo 41 0.042
173
ADJ001 Adjustment Disorder 38 0.042
174
WBR001 Weber Syndrome 37 0.042
175
P PHT010 Photoparoxysmal Response 1 37 0.042
176
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 34 0.042
177
SGT001 Sagittal Sinus Thrombosis 33 0.042
178
c ERL003 Early Onset Absence Epilepsy 23 0.042
179
c SZR016 Seizures, Benign Familial Infantile, 2 22 0.042
180
c CRN174 Coronary Heart Disease 2 22 0.042
181
c DLT002 Dilated Cardiomyopathy 75 0.035
182
WLS001 Wilson Disease 72 0.035
183
ATT013 Attention Deficit-Hyperactivity Disorder 68 0.035
184
CYS013 Cystinuria 63 0.035
185
CRD119 Cardiac Arrest 63 0.035
186
P GRV001 Graves' Disease 61 0.035
187
P THR015 Thrombophilia 59 0.035
188
STT001 Status Epilepticus 59 0.035
189
P PRC031 Preeclampsia/eclampsia 1 57 0.035
190
NRM005 Neuromuscular Disease 57 0.035
191
P INT143 Interstitial Cystitis 57 0.035
192
HYP266 Hypoxia 55 0.035
193
NWC001 Newcastle Disease 54 0.035
194
ALL026 Allergic Hypersensitivity Disease 53 0.035
195
HYP005 Hypokalemia 51 0.035
196
c CNG464 Congenital Myopathy 50 0.035
197
HLL004 Hellp Syndrome 49 0.035
198
CRB090 Cerebral Hypoxia 48 0.035
199
PLN006 Poland Syndrome 48 0.035
200
c PSD066 Pseudohypoparathyroidism, Type Ib 47 0.035
201
PLY012 Polyhydramnios 47 0.035
202
P THY054 Thyrotoxic Periodic Paralysis 47 0.035
203
RNL097 Renal Artery Disease 45 0.035
204
BHR001 Behr Syndrome 44 0.035
205
c HMG003 Hemoglobin E Disease 44 0.035
206
CRD003 Cardiac Sarcoidosis 43 0.035
207
c SZR007 Seizures, Benign Familial Infantile, 3 42 0.035
208
HRT011 Heart Septal Defect 41 0.035
209
IMP006 Impulse Control Disorder 40 0.035
210
MYT011 Myotonia 40 0.035
211
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 37 0.035
212
KHL003 Kohlschutter-Tonz Syndrome 37 0.035
213
INT010 Intracranial Embolism 35 0.035
214
VSC008 Vascular Hemostatic Disease 33 0.035
215
P BNG006 Benign Familial Neonatal Epilepsy 33 0.035
216
c AST039 Asthma 2 31 0.035
217
CRB132 Cerebral Sinovenous Thrombosis 31 0.035
218
PRN033 Paraneoplastic Neurologic Disorders 28 0.035
219
P PRD017 Periodic Paralyses 27 0.035
220
SHP003 Shapiro Syndrome 25 0.035
221
c ALB016 Albinism, Oculocutaneous, Type Vii 24 0.035
222
MND006 Mondor Disease 21 0.035
223
c SZR014 Seizures, Benign Familial Infantile, 1 21 0.035